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Research 211–240 of 1000+
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- <i>Hoxc13</i> mutant mice lack external hair
- An Update of Congenital Adrenal Hyperplasia
- Biology and Genetics of Hair
- Concerted gene duplications in the two keratin gene families
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Congenital hair loss disorders: Rare, but not too rare
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Tuning Wnt Signals for More or Fewer Hairs
- Anabolic-androgenic steroids and cardiovascular risk
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Genetics of Structural Hair Disorders
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Deletion of the <i>Sox21</i> gene drastically affects hair lipids
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy